ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.3915C>T (p.Ser1305=)

dbSNP: rs199830697
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002172765 SCV002339965 likely benign Landau-Kleffner syndrome 2022-10-17 criteria provided, single submitter clinical testing

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